Magnitude of Response With Myeloma Frontline Therapy Does Not Predict Outcome: Importance of Time to Progression in Southwest Oncology Group Chemotherapy Trials

Four Southwest Oncology Group (SWOG) standard-dose chemotherapy protocols for multiple myeloma (MM) initiated between 1982 and 1992 were evaluated. The purpose was to clarify the predictive value of specific levels of myeloma-associated monoclonal protein reduction and time to first progression usin...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of clinical oncology 2004-05, Vol.22 (10), p.1857-1863
Hauptverfasser: DURIE, Brian G. M, JACOBSON, Joth, BARLOGIE, Bart, CROWLEY, John
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1863
container_issue 10
container_start_page 1857
container_title Journal of clinical oncology
container_volume 22
creator DURIE, Brian G. M
JACOBSON, Joth
BARLOGIE, Bart
CROWLEY, John
description Four Southwest Oncology Group (SWOG) standard-dose chemotherapy protocols for multiple myeloma (MM) initiated between 1982 and 1992 were evaluated. The purpose was to clarify the predictive value of specific levels of myeloma-associated monoclonal protein reduction and time to first progression using mature data sets. Study data on 1,555 eligible previously untreated patients with MM enrolled onto SWOG phase III trials 8229, 8624, 9028, and 9210 were used in these analyses. Six-month and 12-month landmark analyses were performed to evaluate the outcome for patients in each response category. The overall and event-free survivals for the four protocols combined were 33 months and 18 months, respectively. Using 6- and 12-month landmarks, the median survivals of 30 to 35 months were not different for responders (> or = 50% and > or = 75% regression) versus nonresponders in patients without disease progression before the landmarks. Conversely, at the 6- and 12-month landmarks, the median survivals for patients who had experienced disease progression were 13 and 15 months, respectively, versus a 34-month median for patients who did not experience progression. Using the Cox survival model, with response and progression considered as time-dependent covariates, survival duration was influenced more by the occurrence of progression than by the occurrence of response. The magnitude of response, as a single variable, does not predict survival duration. Patients with response and stable disease have equivalent outcome. Only patients with progressive disease have a poorer outcome. The best indicator of survival is time to first progression.
doi_str_mv 10.1200/JCO.2004.05.111
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71931788</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71931788</sourcerecordid><originalsourceid>FETCH-LOGICAL-c396t-7886045e3bd57845889ff7126108a6e9538751a50398f8809fa0d55d1bc1b5e53</originalsourceid><addsrcrecordid>eNpNkUFv1DAUhC0EokvhzA35Aj1la8fr2OGGlrYUtSyCRXCzvMnLxlWSF2xH1f4bfipuNxKc5vLNvKcZQl5ztuQ5Y-ef15tl0tWSySXn_AlZcJmrTCkpn5IFUyLPuBa_TsiLEO4Y4yst5HNywmWCC64W5M-t3Q8uTjVQbOg3CCMOAehPF1t6e4AOe0svPQ6xcwPQbQvejgf6ESHQLxjpVw-1qyLdTLHCHt7T635EH-1QPeZtXQ80YsJw7yEEhwN1A_2OU2zvISTfUGGH-wO98jiNdN1Cj3E-svXOduEledYkgVeznpIflxfb9afsZnN1vf5wk1WiLGKmtC7YSoLY1VLpldS6bBrF84IzbQsopdBKciuZKHWjNSsby2opa76r-E6CFKfk3TF39Ph7Sr-Z3oUKus4OgFMwipeCpysJPD-ClccQPDRm9K63_mA4Mw-jmDSKeRjFMGlSz8nxZo6edj3U__h5hQS8nQEbKts1PvXnwn-cKlaFzhN3duRat2_vnQcTett1KTY3dxXm-eMLWirxFwWho2Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>71931788</pqid></control><display><type>article</type><title>Magnitude of Response With Myeloma Frontline Therapy Does Not Predict Outcome: Importance of Time to Progression in Southwest Oncology Group Chemotherapy Trials</title><source>MEDLINE</source><source>American Society of Clinical Oncology Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>DURIE, Brian G. M ; JACOBSON, Joth ; BARLOGIE, Bart ; CROWLEY, John</creator><creatorcontrib>DURIE, Brian G. M ; JACOBSON, Joth ; BARLOGIE, Bart ; CROWLEY, John</creatorcontrib><description>Four Southwest Oncology Group (SWOG) standard-dose chemotherapy protocols for multiple myeloma (MM) initiated between 1982 and 1992 were evaluated. The purpose was to clarify the predictive value of specific levels of myeloma-associated monoclonal protein reduction and time to first progression using mature data sets. Study data on 1,555 eligible previously untreated patients with MM enrolled onto SWOG phase III trials 8229, 8624, 9028, and 9210 were used in these analyses. Six-month and 12-month landmark analyses were performed to evaluate the outcome for patients in each response category. The overall and event-free survivals for the four protocols combined were 33 months and 18 months, respectively. Using 6- and 12-month landmarks, the median survivals of 30 to 35 months were not different for responders (&gt; or = 50% and &gt; or = 75% regression) versus nonresponders in patients without disease progression before the landmarks. Conversely, at the 6- and 12-month landmarks, the median survivals for patients who had experienced disease progression were 13 and 15 months, respectively, versus a 34-month median for patients who did not experience progression. Using the Cox survival model, with response and progression considered as time-dependent covariates, survival duration was influenced more by the occurrence of progression than by the occurrence of response. The magnitude of response, as a single variable, does not predict survival duration. Patients with response and stable disease have equivalent outcome. Only patients with progressive disease have a poorer outcome. The best indicator of survival is time to first progression.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.2004.05.111</identifier><identifier>PMID: 15111617</identifier><language>eng</language><publisher>Baltimore, MD: American Society of Clinical Oncology</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Biomarkers, Tumor - blood ; Clinical Trials, Phase III as Topic ; Disease-Free Survival ; Female ; Hematologic and hematopoietic diseases ; Humans ; Immunodeficiencies. Immunoglobulinopathies ; Immunoglobulinopathies ; Immunopathology ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Male ; Medical sciences ; Middle Aged ; Multiple Myeloma - drug therapy ; Multiple Myeloma - mortality ; Multiple Myeloma - pathology ; Myeloma Proteins - metabolism ; Neoplasm Staging ; Predictive Value of Tests ; Proportional Hazards Models ; Southwestern United States ; Survival Analysis</subject><ispartof>Journal of clinical oncology, 2004-05, Vol.22 (10), p.1857-1863</ispartof><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-7886045e3bd57845889ff7126108a6e9538751a50398f8809fa0d55d1bc1b5e53</citedby><cites>FETCH-LOGICAL-c396t-7886045e3bd57845889ff7126108a6e9538751a50398f8809fa0d55d1bc1b5e53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3729,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=15764682$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15111617$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>DURIE, Brian G. M</creatorcontrib><creatorcontrib>JACOBSON, Joth</creatorcontrib><creatorcontrib>BARLOGIE, Bart</creatorcontrib><creatorcontrib>CROWLEY, John</creatorcontrib><title>Magnitude of Response With Myeloma Frontline Therapy Does Not Predict Outcome: Importance of Time to Progression in Southwest Oncology Group Chemotherapy Trials</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>Four Southwest Oncology Group (SWOG) standard-dose chemotherapy protocols for multiple myeloma (MM) initiated between 1982 and 1992 were evaluated. The purpose was to clarify the predictive value of specific levels of myeloma-associated monoclonal protein reduction and time to first progression using mature data sets. Study data on 1,555 eligible previously untreated patients with MM enrolled onto SWOG phase III trials 8229, 8624, 9028, and 9210 were used in these analyses. Six-month and 12-month landmark analyses were performed to evaluate the outcome for patients in each response category. The overall and event-free survivals for the four protocols combined were 33 months and 18 months, respectively. Using 6- and 12-month landmarks, the median survivals of 30 to 35 months were not different for responders (&gt; or = 50% and &gt; or = 75% regression) versus nonresponders in patients without disease progression before the landmarks. Conversely, at the 6- and 12-month landmarks, the median survivals for patients who had experienced disease progression were 13 and 15 months, respectively, versus a 34-month median for patients who did not experience progression. Using the Cox survival model, with response and progression considered as time-dependent covariates, survival duration was influenced more by the occurrence of progression than by the occurrence of response. The magnitude of response, as a single variable, does not predict survival duration. Patients with response and stable disease have equivalent outcome. Only patients with progressive disease have a poorer outcome. The best indicator of survival is time to first progression.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - blood</subject><subject>Clinical Trials, Phase III as Topic</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Immunodeficiencies. Immunoglobulinopathies</subject><subject>Immunoglobulinopathies</subject><subject>Immunopathology</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multiple Myeloma - drug therapy</subject><subject>Multiple Myeloma - mortality</subject><subject>Multiple Myeloma - pathology</subject><subject>Myeloma Proteins - metabolism</subject><subject>Neoplasm Staging</subject><subject>Predictive Value of Tests</subject><subject>Proportional Hazards Models</subject><subject>Southwestern United States</subject><subject>Survival Analysis</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkUFv1DAUhC0EokvhzA35Aj1la8fr2OGGlrYUtSyCRXCzvMnLxlWSF2xH1f4bfipuNxKc5vLNvKcZQl5ztuQ5Y-ef15tl0tWSySXn_AlZcJmrTCkpn5IFUyLPuBa_TsiLEO4Y4yst5HNywmWCC64W5M-t3Q8uTjVQbOg3CCMOAehPF1t6e4AOe0svPQ6xcwPQbQvejgf6ESHQLxjpVw-1qyLdTLHCHt7T635EH-1QPeZtXQ80YsJw7yEEhwN1A_2OU2zvISTfUGGH-wO98jiNdN1Cj3E-svXOduEledYkgVeznpIflxfb9afsZnN1vf5wk1WiLGKmtC7YSoLY1VLpldS6bBrF84IzbQsopdBKciuZKHWjNSsby2opa76r-E6CFKfk3TF39Ph7Sr-Z3oUKus4OgFMwipeCpysJPD-ClccQPDRm9K63_mA4Mw-jmDSKeRjFMGlSz8nxZo6edj3U__h5hQS8nQEbKts1PvXnwn-cKlaFzhN3duRat2_vnQcTett1KTY3dxXm-eMLWirxFwWho2Q</recordid><startdate>20040515</startdate><enddate>20040515</enddate><creator>DURIE, Brian G. M</creator><creator>JACOBSON, Joth</creator><creator>BARLOGIE, Bart</creator><creator>CROWLEY, John</creator><general>American Society of Clinical Oncology</general><general>Lippincott Williams &amp; Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20040515</creationdate><title>Magnitude of Response With Myeloma Frontline Therapy Does Not Predict Outcome: Importance of Time to Progression in Southwest Oncology Group Chemotherapy Trials</title><author>DURIE, Brian G. M ; JACOBSON, Joth ; BARLOGIE, Bart ; CROWLEY, John</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-7886045e3bd57845889ff7126108a6e9538751a50398f8809fa0d55d1bc1b5e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - blood</topic><topic>Clinical Trials, Phase III as Topic</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Immunodeficiencies. Immunoglobulinopathies</topic><topic>Immunoglobulinopathies</topic><topic>Immunopathology</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multiple Myeloma - drug therapy</topic><topic>Multiple Myeloma - mortality</topic><topic>Multiple Myeloma - pathology</topic><topic>Myeloma Proteins - metabolism</topic><topic>Neoplasm Staging</topic><topic>Predictive Value of Tests</topic><topic>Proportional Hazards Models</topic><topic>Southwestern United States</topic><topic>Survival Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DURIE, Brian G. M</creatorcontrib><creatorcontrib>JACOBSON, Joth</creatorcontrib><creatorcontrib>BARLOGIE, Bart</creatorcontrib><creatorcontrib>CROWLEY, John</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DURIE, Brian G. M</au><au>JACOBSON, Joth</au><au>BARLOGIE, Bart</au><au>CROWLEY, John</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Magnitude of Response With Myeloma Frontline Therapy Does Not Predict Outcome: Importance of Time to Progression in Southwest Oncology Group Chemotherapy Trials</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2004-05-15</date><risdate>2004</risdate><volume>22</volume><issue>10</issue><spage>1857</spage><epage>1863</epage><pages>1857-1863</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>Four Southwest Oncology Group (SWOG) standard-dose chemotherapy protocols for multiple myeloma (MM) initiated between 1982 and 1992 were evaluated. The purpose was to clarify the predictive value of specific levels of myeloma-associated monoclonal protein reduction and time to first progression using mature data sets. Study data on 1,555 eligible previously untreated patients with MM enrolled onto SWOG phase III trials 8229, 8624, 9028, and 9210 were used in these analyses. Six-month and 12-month landmark analyses were performed to evaluate the outcome for patients in each response category. The overall and event-free survivals for the four protocols combined were 33 months and 18 months, respectively. Using 6- and 12-month landmarks, the median survivals of 30 to 35 months were not different for responders (&gt; or = 50% and &gt; or = 75% regression) versus nonresponders in patients without disease progression before the landmarks. Conversely, at the 6- and 12-month landmarks, the median survivals for patients who had experienced disease progression were 13 and 15 months, respectively, versus a 34-month median for patients who did not experience progression. Using the Cox survival model, with response and progression considered as time-dependent covariates, survival duration was influenced more by the occurrence of progression than by the occurrence of response. The magnitude of response, as a single variable, does not predict survival duration. Patients with response and stable disease have equivalent outcome. Only patients with progressive disease have a poorer outcome. The best indicator of survival is time to first progression.</abstract><cop>Baltimore, MD</cop><pub>American Society of Clinical Oncology</pub><pmid>15111617</pmid><doi>10.1200/JCO.2004.05.111</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0732-183X
ispartof Journal of clinical oncology, 2004-05, Vol.22 (10), p.1857-1863
issn 0732-183X
1527-7755
language eng
recordid cdi_proquest_miscellaneous_71931788
source MEDLINE; American Society of Clinical Oncology Journals; EZB-FREE-00999 freely available EZB journals
subjects Adult
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Biomarkers, Tumor - blood
Clinical Trials, Phase III as Topic
Disease-Free Survival
Female
Hematologic and hematopoietic diseases
Humans
Immunodeficiencies. Immunoglobulinopathies
Immunoglobulinopathies
Immunopathology
Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
Male
Medical sciences
Middle Aged
Multiple Myeloma - drug therapy
Multiple Myeloma - mortality
Multiple Myeloma - pathology
Myeloma Proteins - metabolism
Neoplasm Staging
Predictive Value of Tests
Proportional Hazards Models
Southwestern United States
Survival Analysis
title Magnitude of Response With Myeloma Frontline Therapy Does Not Predict Outcome: Importance of Time to Progression in Southwest Oncology Group Chemotherapy Trials
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T17%3A13%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Magnitude%20of%20Response%20With%20Myeloma%20Frontline%20Therapy%20Does%20Not%20Predict%20Outcome:%20Importance%20of%20Time%20to%20Progression%20in%20Southwest%20Oncology%20Group%20Chemotherapy%20Trials&rft.jtitle=Journal%20of%20clinical%20oncology&rft.au=DURIE,%20Brian%20G.%20M&rft.date=2004-05-15&rft.volume=22&rft.issue=10&rft.spage=1857&rft.epage=1863&rft.pages=1857-1863&rft.issn=0732-183X&rft.eissn=1527-7755&rft_id=info:doi/10.1200/JCO.2004.05.111&rft_dat=%3Cproquest_cross%3E71931788%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=71931788&rft_id=info:pmid/15111617&rfr_iscdi=true